DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
IBUPROFEN
FDA Application No:
(ANDA) 071335
Active Ingredient(s):
IBUPROFEN
Company:
INTERPHARM
Label History
Labels are not available on this site for IBUPROFEN, (ANDA) 071335
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
9/25/2001
025
Manufacturing Revision
4/12/2000
024
Manufacturing Revision
4/12/2000
023
Control Supplement
8/30/1999
022
Labeling
4/12/2000
021
Facility Addition
9/24/1999
019
Chemistry
2/11/1999
018
Chemistry
7/24/1997
017
Chemistry
1/20/1998
015
Chemistry
1/30/1992
014
Labeling
1/19/1989
013
Labeling
10/11/1988
012
Labeling
7/26/1988
010
Chemistry
3/28/1988
010
Labeling
4/5/1988
009
Chemistry
4/5/1988
008
Chemistry
4/5/1988
007
Chemistry
1/7/1988
005
Chemistry
1/12/1988
004
Chemistry
10/8/1987
003
Chemistry
6/24/1987
001
Chemistry
11/25/1986
000
Approval
Therapeutic Equivalents
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